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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963151Generated: October 29, 2026

N,N-Dimethylaniline → 2-Benzylthio-5-chloro-7-methyl[1,2,4]triazolo[1,5-a]pyridine

https://huagongshe.com/reaction/963151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
ReactantHexaneHCID 8058—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178429177HCID 178429177—
SolventEthyl AcetateHCID 8857—
Product2-Benzylthio-5-chloro-7-methyl[1,2,4]triazolo[1,5-a]pyridineHCID 19080764—

Reaction Steps

N,N-Dimethylaniline (21.9 g, 0.18 mol) was added slowly to a mixture of 2-benzylthio-5-hydroxy-7-methyl[1,2,4]triazolo[1,5-a]pyridine (44.5 g, 0.164 mol) in 150 mL of phosphorus oxychloride with stirring. The mixture was heated at reflux with stirring for 20 hours. The excess phosphorus oxychloride was then removed by evaporation under reduced pressure. The residue obtained was dissolved in ethyl acetate, washed well with water and quickly concentrated by evaporation under reduced pressure to drive off the excess water. The residue was again dissolved in ethyl acetate and the resulting mixture was filtered with suction through a bed of silica gel. The filtrate was concentrated by evaporation under reduced pressure and the residue obtained was mixed with hexane. The resulting mixture was filtered to recover the solids and dried to obtain the 37.5 g (79 percent of theory) of the title compound as a tan powder melting at 108°-110° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763359
Source datasetuspto-grants-1998_06
ORD IDord-de1aa12c8194405082ff58e61bf4434f
Source noteuspto-grants-1998_06